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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912589copy number variation1nstd209human GRCh38 chr9: 27,194,806-27,296,013 , GRCh37.p13 chr9: 27,194,804-27,296,011 EQTN, RPL36AP34, 3 more genes
    nsv5852477copy number variation1nstd209human GRCh38 chr9: 27,283,974-27,289,398 , GRCh37.p13 chr9: 27,283,972-27,289,396 EQTN
    nsv5849955copy number variation1nstd209human GRCh38 chr9: 27,274,047-27,289,398 , GRCh37.p13 chr9: 27,274,045-27,289,396 EQTN, LINC00032
    nsv5847887copy number variation1nstd209human GRCh38 chr9: 27,274,021-27,295,398 , GRCh37.p13 chr9: 27,274,019-27,295,396 LINC00032, EQTN
    nsv5488996copy number variation1nstd206human GRCh38 chr9: 27,194,806-27,296,018 , GRCh37.p13 chr9: 27,194,804-27,296,016 TEK, RPL36AP34, 3 more genes
    nsv5484580copy number variation1nstd206human GRCh38 chr9: 27,283,624-27,289,707 , GRCh37.p13 chr9: 27,283,622-27,289,705 EQTN
    nsv5127834mobile element insertion1nstd203human GRCh38 chr9: 27,295,361-27,295,376 , GRCh37.p13 chr9: 27,295,359-27,295,374 EQTN
    nsv4954600copy number variation1nstd200human GRCh38 chr9: 27,220,362-27,288,686 , GRCh37.p13 chr9: 27,220,360-27,288,684 LINC00032, EQTN, 1 more genes
    nsv4954598copy number variation1nstd200human GRCh38 chr9: 27,194,806-27,296,018 , GRCh37.p13 chr9: 27,194,804-27,296,016 RPL36AP34, LINC00032, 3 more genes
    nsv4814708copy number variation1nstd200human GRCh37 chr9: 27,194,804-27,296,016 , GRCh38.p12 chr9: 27,194,806-27,296,018 TEK, RPL36AP34, 3 more genes
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4745683copy number variation1nstd199human GRCh37 chr9: 6,727,606-30,688,993 , GRCh38.p12 chr9: 6,727,606-30,688,995 , RPS6P10, 230 more genes
    nsv4729689copy number variation1nstd102humanUncertain significance GRCh37 chr9: 26,461,273-27,541,041 , GRCh38.p12 chr9: 26,461,275-27,541,043 IFT74, PLAA, 15 more genes
    nsv4728999copy number variation1nstd102humanUncertain significance GRCh37 chr9: 26,545,337-27,494,803 , GRCh38.p12 chr9: 26,545,339-27,494,805 LOC107987028, TEK, 13 more genes
    nsv4679043copy number variation1nstd189human GRCh37.p13 chr9: 26,629,345-27,609,646 , GRCh38.p12 chr9: 26,629,347-27,609,648 , TEK, 19 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4617660copy number variation1nstd183human GRCh37 chr9: 26,347,303-27,646,992 , GRCh38.p12 chr9: 26,347,305-27,646,994 , RNA5SP280, 21 more genes
    nsv4601277copy number variation1nstd183human GRCh37 chr9: 27,279,627-27,343,573 , GRCh38.p12 chr9: 27,279,629-27,343,575 EQTN, MOB3B, 1 more genes
    nsv4551262insertion1nstd166human GRCh37.p13 chr9: 27,291,663-27,291,663 , GRCh38.p12 chr9: 27,291,665-27,291,665 EQTN
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